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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730732Generated: October 31, 2026

Hydrochloric Acid → HCID 53654790, compound

https://huagongshe.com/reaction/1730732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl ThioglycolateHCID 16907—
Reactant1-[4-(2-fluorophenyl)phenyl]propan-1-olHCID 2741170—
Reactant4-(1-chloropropyl)-2'-fluoro-1,1'-biphenylHCID 2781685—
ReactantSodium borohydrideHCID 4311764—
ReactantPotassiumHCID 5462222—
ReactantHCID 53921419HCID 53921419—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 53654790HCID 53654790—

Reaction Steps

101.5 gm (0.905 mol) of potassium tert.butylate, suspended in 500 ml of dimethylformamide, were admixed, while stirring and cooling under exclusion of air, with 96.0 gm (0.905 mol) of thioglycolic acid methyl ester. To the solution of the potassium salt, the mixture was admixed with 205.9 gm (0.822 mol) of 1-chloro-1-(2'-fluoro-4-biphenylyl)-propane [prepared by reduction of 2'-fluoro-4-biphenylyl-ethylketone with sodium borohydride and subsequent reaction of the obtained 1-hydroxy-1-(2'-fluoro-4-biphenylyl)-propane with hydrochloric acid in benzene], and the mixture was stirred for 4 hours at room temperature. Subsequently, 2 liters of water were added, and the reaction product was isolated by extraction with ethyl acetate, and washing, drying and evaporating of the extract. Yield: 254 gm (97% of theory); oil, Rf -value: 0.5 (cyclohexane-ethyl acetate = 9:1 on silicagelpolygram-plates).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03993683
Source datasetuspto-grants-1976_11
ORD IDord-b756828650564546ac5664c2b875584c
Source noteuspto-grants-1976_11